4 years ago

HPV16 E7 Genetic Conservation Is Critical to Carcinogenesis

HPV16 E7 Genetic Conservation Is Critical to Carcinogenesis
Joan Walker, Carolina Porras, Chase W. Nelson, Nicolas Wentzensen, Lei Song, Mark Schiffman, Robert D. Burk, Joseph F. Boland, Michael Dean, Daniel C. Beachler, Aimée R. Kreimer, Rosemary Zuna, Laurie Burdett, Silvia Franceschi, Zigui Chen, Qi Yang, Yanzi Xiao, Paula Gonzalez, Bin Zhu, Meredith Yeager, Mia Steinberg, Philip E. Castle, Jason Mitchell, David Roberson, Gary M. Clifford, Allan Hildesheim, Tina Raine-Bennett, Kai Yu, Michael Cullen, Lisa Mirabello, Sara Bass, Thomas Lorey


Although most cervical human papillomavirus type 16 (HPV16) infections become undetectable within 1–2 years, persistent HPV16 causes half of all cervical cancers. We used a novel HPV whole-genome sequencing technique to evaluate an exceptionally large collection of 5,570 HPV16-infected case-control samples to determine whether viral genetic variation influences risk of cervical precancer and cancer. We observed thousands of unique HPV16 genomes; very few women shared the identical HPV16 sequence, which should stimulate a careful re-evaluation of the clinical implications of HPV mutation rates, transmission, clearance, and persistence. In case-control analyses, HPV16 in the controls had significantly more amino acid changing variants throughout the genome. Strikingly, E7 was devoid of variants in precancers/cancers compared to higher levels in the controls; we confirmed this in cancers from around the world. Strict conservation of the 98 amino acids of E7, which disrupts Rb function, is critical for HPV16 carcinogenesis, presenting a highly specific target for etiologic and therapeutic research.

Publisher URL: http://www.cell.com/cell/fulltext/S0092-8674(17)30889-9

DOI: 10.1016/j.cell.2017.08.001

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